Product Recalls in New Mexico
Product recalls affecting New Mexico — including food, drugs, consumer products, medical devices, and vehicles distributed to New Mexico. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,699 recalls have been distributed to New Mexico in the last 12 months.
Showing 45961–45980 of 48,595 recalls
Recalled Item: Well at Walgreens Wal-Tussin CF Max Recalled by Aaron Industries Inc Due to...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Select Brand Cough Control CF Max Recalled by Aaron Industries Inc Due to...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Wal-Mart Equate Tussin CF Adult Maximum Strength Recalled by Aaron...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rite Aid Maximum Strength Tussin Cough & Cold Mucus Relief CF Recalled by...
The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and...
The Issue: Microbial Contamination of Non-Sterile Product(s): The product has the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SybronEndo Replacement AC Power Cord Recalled by Ormco/Sybronendo Due to A...
The Issue: A recall has been issued by SybronEndo because a Canadian Standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SybronEndo Elements Obturation Unit Recalled by Ormco/Sybronendo Due to A...
The Issue: A recall has been issued by SybronEndo because a Canadian Standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KODAK INSIGHT DENTAL FILM in SureSoft Packets Recalled by Carestream Health,...
The Issue: Missing symbols and manufacturing information on the clear carton label. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tausi Brand Salted Black Beans Recalled by Walong Marketing, Inc. Due to...
The Issue: Walong is recalling Tausi Brand Salted Black Beans because it may have the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Tausi Brand Salted Black Beans Recalled by G.L. Food Wholesale Inc Due to GL...
The Issue: GL Food Wholesale is recalling Tausi Brand Salted Black Beans because it may...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Philips BuckyDiagnost Radiographic. Catalog Numbers: 704031 Recalled by...
The Issue: An inspection of IATD (Installation Acceptance Test Document)IA SID (Source...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...
The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips BuckyDiagnost Radiographic Recalled by Philips Healthcare Inc. Due...
The Issue: An inspection shows several IATDs (Installation Acceptance Test could not be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phillips Easy Diagnost Eleva DRF. Model Number: 706034 Product Usage:...
The Issue: The mirror icon on the bottom of each image could be misinterpreted as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...
The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Product exceeds specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Iconos R200 C20 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens has become aware of a potential malfunction and possible hazard to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT Catalog Number:283905000....
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 7CC KIT Catalog Number: 283907000....
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs BleaseSirius Anesthesia Workstation Recalled by Del Mar Reynolds...
The Issue: A defect in CAS I/II Absorbers in the Spacelabs Anesthesia Workstations and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.